Diode Laser Plus CPP-ACPF vs CPP-ACPF Alone for Dentin Hypersensitivity
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-50
SponsorCairo University
About this trial
This study aims to compare the effectiveness of diode laser photobiomodulation combined with CPP-ACPF varnish versus CPP-ACPF varnish alone in reducing dentin hypersensitivity. Participants diagnosed with dentin hypersensitivity will receive either the combined treatment or varnish application alone. Pain levels will be evaluated using a standardized visual analog scale before and after treatment sessions. The results of this study may help determine whether adding diode laser therapy enhances the effectiveness of conventional varnish treatment in managing dentin hypersensitivity.
Eligibility criteria
Qualifiers
Adult participants aged from 20 to 50 years of age.
Participants with good oral hygiene.
Presence of at least one tooth with dentin hypersensitivity confirmed by the air blast and/or tactile stimuli (scoring ≥3 on the VAS).
Participants willing to cooperate and attend recall appointments
Disqualifiers
Participants with poor oral hygiene.
History of professional or at-home desensitizing treatment within the previous 3 months.
Pregnant or lactating females.
Concurrent participation in other research studies.
Trial design
Treatments tested in this trial
- Diode laser photobiomodulation combined with CPP-ACPF varnish
- CPP-ACPF varnish
Treatment groups
70 Participants
are divided into 2 treatment groupsLocations
Sponsors and collaborators
Source ClinicalTrials.gov